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Ritsuko Sasaki

Researcher at Juntendo University

Publications -  10
Citations -  64

Ritsuko Sasaki is an academic researcher from Juntendo University. The author has contributed to research in topics: Breast cancer & Internal medicine. The author has an hindex of 3, co-authored 6 publications receiving 25 citations.

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Microsatellite instability and mismatch repair protein expressions in lymphocyte‐predominant breast cancer

TL;DR: Tests on triple‐negative breast cancers with a high density of tumor‐infiltrating lymphocytes found that MSI‐H tumors were absent in TIL‐high breast cancers, and examination of MMR proteins and PD‐L1 expression may merit further studies to yield predictive information for identifying patients who are likely to benefit from ICI.
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Neutrophil-to-lymphocyte ratio and histological type might predict clinical responses to eriburin-based treatment in patients with metastatic breast cancer.

TL;DR: Predictive markers for eribulin-based treatment responsiveness in patients with MBC are investigated by examining clinicopathological features, including several markers of immunocompetent cells in peripheral blood, which revealed that special histological types and high NLR might be factors related to low responsiveness to eribul-based regimens in patientsWith MBC.
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High FOXA1 protein expression might predict late recurrence in patients with estrogen-positive and HER2-negative breast cancer

TL;DR: The data are raised to raise the possibility of forkhead box A1 being a useful predictive marker for late recurrence and to provide new insights into the biology of FOXA1-high breast cancers.
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High platelet-to-lymphocyte ratios in triple-negative breast cancer associates with immunosuppressive status of TILs

TL;DR: In this paper , the authors investigated the relationship between TILs and the peripheral blood markers, platelet-to-lymphocyte ratios (PLRs) and neutrophil-tolymphocytes ratios (NLRs), in the same patients, using surgical specimens from 502 patients with invasive breast carcinoma without preoperative chemotherapy.
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Estrogen Receptor-positive Ductal Carcinoma In Situ Frequently Overexpresses HER2 Protein Without Gene Amplification.

TL;DR: It is revealed that ER(+) and HER2 protein-overexpressing DCIS, especially ER-high tumors, frequently overexpress HER2protein without gene amplification, which may provide novel insights for understanding the biology of DCIS.